Atypical morphologic presentation of biliary atresia and value of serial liver biopsies

被引:65
作者
Azar, G
Beneck, D
Lane, B
Markowitz, J
Daum, F
Kahn, E
机构
[1] NYU, Sch Med, N Shore Univ Hosp, Dept Pathol, Manhasset, NY 11030 USA
[2] NYU, Sch Med, N Shore Univ Hosp, Dept Pediat, Manhasset, NY 11030 USA
[3] New York Med Coll, Dept Pathol, Valhalla, NY 10595 USA
[4] SUNY Stony Brook, Dept Pathol, Stony Brook, NY 11794 USA
关键词
biliary atresia; biliary tract; children; conjugated hyperbilirubinemia; biliary obstruction; paucity of intrahepatic bile ducts;
D O I
10.1097/00005176-200202000-00020
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Liver biopsy findings are important in diagnosing extrahepatic biliary atresia. Diffuse ductular proliferation is a characteristic finding. We describe four patients with conjugated hyperbilirubinemia in whom the initial liver biopsy findings showed a lack of ductular proliferation. despite subsequent development of biliary atresia. Results: On initial biopsy. paucity of intrahepatic bile ducts was present in three of four patients. with a bile duct to portal space ratio of 0.3 to 0.4 (normal, 0.9-1.8). A normal bile duct to portal space ratio of 1.0 was observed in the fourth patient. Ductular proliferation became apparent in three Subjects between 9 and 12 weeks of age. and biliary atresia was noted at the time of a Kasai portoenterostomy. The fourth child had well-developed biliary cirrhosis at liver transplantation. Conclusions: Changes characteristic of biliary atresia may appear even after 9 weeks of age. Bile duct paucity and normal bile duct to portal space ratio do not preclude the subsequent development of biliary atresia. Infants with unexplained conjugated hyperbilirubinemia and acholic stools should undergo sequential liver biopsies until clinical improvement occurs or until biliary atresia call be excluded from the differential diagnosis.
引用
收藏
页码:212 / 215
页数:4
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